Canonical Allele Identifier: CA2374743089

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350658G= , CM000682.2:g.63350658G=	GRCh38
NC_000020.10:g.61982010G= , CM000682.1:g.61982010G=	GRCh37
NC_000020.9:g.61452454G=	NCBI36
NG_011931.1:g.15686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.753C= MANE Select	ENSP00000359285.4:p.Ile251=
ENST00000370263.8:c.753C=	ENSP00000359285.4:p.Ile251=
ENST00000463705.5:n.1401C=
ENST00000467563.3:n.823C=
ENST00000498043.6:c.777C=
ENST00000615287.4:c.540C=	ENSP00000483388.1:p.Ile180=
ENST00000627000.1:c.*442C=	ENSP00000486914.1:n.*442C=
ENST00000630240.1:n.474C=
NM_000744.6:c.753C=	NP_000735.1:p.Ile251=
NM_001256573.1:c.225C=	NP_001243502.1:p.Ile75=
NR_046317.1:n.1009C=
XM_011528524.1:c.540C=	XP_011526826.1:p.Ile180=
XM_017027625.2:c.225C=	XP_016883114.1:p.Ile75=
XM_024451822.1:c.225C=	XP_024307590.1:p.Ile75=
NM_001256573.2:c.225C=	NP_001243502.1:p.Ile75=
NR_046317.2:n.962C=
NM_000744.7:c.753C= MANE Select	NP_000735.1:p.Ile251=